Prevention of Maternal-fetal Cytomegalovirus Transmission After Primary Maternal Infection, GW ≤ … (NCT05170269) | Clinical Trial Compass
TerminatedPhase 3
Prevention of Maternal-fetal Cytomegalovirus Transmission After Primary Maternal Infection, GW ≤ 14 (PreCyssion)
Stopped: Sponsor decision
Germany48 participantsStarted 2021-11-17
Plain-language summary
A phase 3, open-label, single-arm, prospective, multi-center trial of Cytotect CP Biotest (BT097) for prevention of maternal-fetal CMV transmission after primary maternal CMV infection. The main purpose of the trial is to demonstrate efficacy and safety of Cytotect CP Biotest in preventing maternal-fetal transmission of cytomegalovirus (CMV).
Who can participate
Age range18 Years – 45 Years
SexFEMALE
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Inclusion Criteria:
* Written informed consent obtained from subjects indicating that they understand the purpose of and procedures required for the trial and are willing to participate in it
* Pregnant women, age 18 to 45 years
* Pregnant women at trial entry with gestational age ≤14 weeks; pregnancy after in-vitro fertilization permitted
* Detection of early primary CMV infection
Exclusion Criteria:
* Women with current multiple pregnancy
* History of severe pre-eclampsia or severe gestational hypertension (GHTN), which required medical intervention. Definition according to AWMF guideline (AWMF, 2019)
* Presence of severe disease impairing course of pregnancy (e.g. diabetes, epilepsy, cancer)
* Congenital or acquired autoimmune disease
* Known immunosuppressive (e.g., transplanted patients) or immunodeficient condition
* Known infection with hepatitis B or C, or HIV from the medical history or active infection at screening as assessed by respective virus serology
* Maternal CMV infection prior to this pregnancy (preconceptional CMV infection)
* Covid-19 infection at time of inclusion
* Any signs or symptoms indicating an increased risk of abortion or premature labor or has known negative effect on fetus with exception of a CMV infection
* Active infection according to TORCH serology with exception of CMV in the assessment of the investigator
* Known major fetal anomalies or demise
* Intolerance to proteins of human origin or known allergic reactions to components of the …
What they're measuring
1
To determine the overall rate of maternal-fetal transmission at the time of amniocentesis (week 20 [-1 week / +2 weeks] of gestation)